被盖腹侧区
神经科学
前额叶皮质
多巴胺
多巴胺能
神经肽
心理学
神经元
抑制性突触后电位
内科学
受体
医学
认知
作者
Bernardo Stutz,Michael Waterson,Matija Šestan-Peša,Marcelo O. Dietrich,Mario Škarica,Nenad Šestan,Bence Rácz,Aletta Magyar,Péter Sótonyi,Liu Hon,Xiao‐Bing Gao,Ferenc Mátyás,Milan Stoiljković,Tamas L. Horváth
标识
DOI:10.1038/s41380-022-01691-8
摘要
Hypothalamic agouti-related peptide and neuropeptide Y-expressing (AgRP) neurons have a critical role in both feeding and non-feeding behaviors of newborn, adolescent, and adult mice, suggesting their broad modulatory impact on brain functions. Here we show that constitutive impairment of AgRP neurons or their peripubertal chemogenetic inhibition resulted in both a numerical and functional reduction of neurons in the medial prefrontal cortex (mPFC) of mice. These changes were accompanied by alteration of oscillatory network activity in mPFC, impaired sensorimotor gating, and altered ambulatory behavior that could be reversed by the administration of clozapine, a non-selective dopamine receptor antagonist. The observed AgRP effects are transduced to mPFC in part via dopaminergic neurons in the ventral tegmental area and may also be conveyed by medial thalamic neurons. Our results unmasked a previously unsuspected role for hypothalamic AgRP neurons in control of neuronal pathways that regulate higher-order brain functions during development and in adulthood.
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